ClinGen Allele Registry
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Canonical Allele Identifier:
CA162971857
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.95404734C>G
GRCh37
chr7:g.95034046C>G
Linked Data - Sequence & Population
gnomAD v2:
7:95034046 C / G
gnomAD v3:
7:95404734 C / G
gnomAD v4:
chr7-95404734-C-G
Joint Max Group AF
0.04785265 (AFR)
Genomes Max Group AF
0.04785493 (AFR)
Exomes Max Group AF
0.00987094 (AMR)
Linked Data - NCBI & NCI
dbSNP:
13306702
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.95404734C>G , CM000669.2:g.95404734C>G
GRCh38
NC_000007.13:g.95034046C>G , CM000669.1:g.95034046C>G
GRCh37
NC_000007.12:g.94871982C>G
NCBI36
NG_008725.1:g.35339G>C
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